Effects of CYP3A4*1G and CYP3A5*3 polymorphisms on pharmacokinetics of tylerdipine hydrochloride in healthy Chinese subjects
Author:
Affiliation:
1. Phase I Clinical Trial Unit, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China;
2. Key Laboratory of Drug Metabolism and Pharmacokinetics, China Pharmaceutical University, Nanjing, China
Funder
XuanZhu Pharma Co., Ltd.
Publisher
Informa UK Limited
Subject
Health, Toxicology and Mutagenesis,Pharmacology,Toxicology,Biochemistry,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/00498254.2018.1447711
Reference27 articles.
1. Substrate-specific modulation of CYP3A4 activity by genetic variants of cytochrome P450 oxidoreductase
2. Heterogeneity of L- and T-Channels in the Vasculature
3. Significance of the Minor Cytochrome P450 3A Isoforms
4. Pharmacogenomics — Drug Disposition, Drug Targets, and Side Effects
5. CYP3A4*1G polymorphism is associated with lipid-lowering efficacy of atorvastatin but not of simvastatin
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